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rs397509025

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509025(-;-)
Make rs397509025(-;CC)
Make rs397509025(CC;CC)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092600
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509025
ebirs397509025
HLIrs397509025
Exacrs397509025
Varsomers397509025
Maprs397509025
PheGenIrs397509025
hapmaprs397509025
1000 genomesrs397509025
hgdprs397509025
ensemblrs397509025
gopubmedrs397509025
geneviewrs397509025
scholarrs397509025
googlers397509025
pharmgkbrs397509025
gwascentralrs397509025
openSNPrs397509025
23andMers397509025
23andMe allrs397509025
SNP Nexus

SNPshotrs397509025
SNPdbers397509025
MSV3drs397509025
GWAS Ctlgrs397509025
Max Magnitude0
ClinVar
Risk rs397509025(CC;CC)
Alt rs397509025(CC;CC)
Reference rs397509025(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244618_41244619dupGG
CLNSRC ClinVar
CLNACC RCV000048014.2,